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B B De Vries

Showing results (11-20 of 23) with videos related to

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Journal of Medical Genetics|September 1, 1993
Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotypeB B de Vries, J P Fryns, M G Butler, et al.
Human Molecular Genetics|January 1, 1994
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11Y Q Wu, P Heutink, B B de Vries, et al.
American Journal of Medical Genetics|October 26, 1999
Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14)B B de Vries, B H Eussen, O P van Diggelen, et al.
American Journal of Medical Genetics|July 15, 1994
DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 geneA M van den Ouweland, B B de Vries, P L Bakker, et al.
Journal of Medical Genetics|June 30, 2000
Screening for the fragile X syndrome among the mentally retarded: a clinical study. The Collaborative Fragile X Study GroupB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
Journal of Medical Genetics|December 1, 1996
Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X familyB B de Vries, C C Jansen, A A Duits, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Mental status and fragile X expression in relation to FMR-1 gene mutationB B de Vries, A M Wiegers, E de Graaff, et al.
American Journal of Human Genetics|October 27, 1997
Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study GroupB B de Vries, A M van den Ouweland, S Mohkamsing, et al.
American Journal of Human Genetics|May 1, 1996
Mental status of females with an FMR1 gene full mutationB B de Vries, A M Wiegers, A P Smits, et al.
Prenatal Diagnosis|July 23, 1999
First-trimester diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) using PPT enzyme assay and CLN1 mutation analysisB B de Vries, W J Kleijer, J L Keulemans, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|September 1, 1993
Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotypeB B de Vries, J P Fryns, M G Butler, et al.
Human Molecular Genetics|January 1, 1994
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11Y Q Wu, P Heutink, B B de Vries, et al.
American Journal of Medical Genetics|October 26, 1999
Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14)B B de Vries, B H Eussen, O P van Diggelen, et al.
American Journal of Medical Genetics|July 15, 1994
DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 geneA M van den Ouweland, B B de Vries, P L Bakker, et al.
Journal of Medical Genetics|June 30, 2000
Screening for the fragile X syndrome among the mentally retarded: a clinical study. The Collaborative Fragile X Study GroupB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
Journal of Medical Genetics|December 1, 1996
Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X familyB B de Vries, C C Jansen, A A Duits, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Mental status and fragile X expression in relation to FMR-1 gene mutationB B de Vries, A M Wiegers, E de Graaff, et al.
American Journal of Human Genetics|October 27, 1997
Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study GroupB B de Vries, A M van den Ouweland, S Mohkamsing, et al.
American Journal of Human Genetics|May 1, 1996
Mental status of females with an FMR1 gene full mutationB B de Vries, A M Wiegers, A P Smits, et al.
Prenatal Diagnosis|July 23, 1999
First-trimester diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) using PPT enzyme assay and CLN1 mutation analysisB B de Vries, W J Kleijer, J L Keulemans, et al.
Pageof 3